Synthesis and biological evaluation of (−)-laulimalide analogues
- 9 February 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (3) , 575-579
- https://doi.org/10.1016/j.bmcl.2003.12.001
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- The Microtubule Stabilizing Agent Laulimalide Does Not Bind in the Taxoid Site, Kills Cells Resistant to Paclitaxel and Epothilones, and May Not Require Its Epoxide Moiety for ActivityBiochemistry, 2002
- Total Synthesis of Microtubule-Stabilizing Agent (−)-Laulimalide1The Journal of Organic Chemistry, 2001
- An Intramolecular Case of Sharpless Kinetic Resolution: Total Synthesis of LaulimalideAngewandte Chemie International Edition in English, 2001
- Total Synthesis of the Microtubule-Stabilizing Agent (−)-LaulimalideOrganic Letters, 2001
- A macrolactonization-based strategy to obtain microtuble-stabilizing agent (−)-laulimalideTetrahedron Letters, 2001
- Total Synthesis of (−)-LaulimalideJournal of the American Chemical Society, 2000
- New Cytotoxic Macrolides from the Sponge Fasciospongia rimosaChemistry Letters, 1996
- Structures and absolute configurations of the marine toxins, latrunculin A and laulimalideTetrahedron Letters, 1996
- Laulimalides. New potent cytotoxic macrolides from a marine sponge and a nudibranch predatorThe Journal of Organic Chemistry, 1988
- Fijianolides, polyketide heterocycles from a marine spongeThe Journal of Organic Chemistry, 1988